Zobrazeno 1 - 10
of 239
pro vyhledávání: '"Vincenzo Santinelli"'
Autor:
Carlo Pappone, Vincenzo Santinelli
Publikováno v:
Arrhythmia & Electrophysiology Review, Vol 8, Iss 1, Pp 13-18 (2019)
Externí odkaz:
https://doaj.org/article/8d7175cab62b4375b427ec6ea14051a5
Autor:
Emanuele Micaglio, Michelle M. Monasky, Giuseppe Ciconte, Gabriele Vicedomini, Manuel Conti, Valerio Mecarocci, Luigi Giannelli, Federica Giordano, Alberto Pollina, Massimo Saviano, Paolo R. Pozzi, Chiara Di Resta, Sara Benedetti, Maurizio Ferrari, Vincenzo Santinelli, Carlo Pappone
Publikováno v:
Frontiers in Genetics, Vol 10 (2019)
In this case report, we characterize a novel inherited frameshift mutation c.4700_4701del (p.Phe1567Cysfs*221) in a single copy of the SCN5A gene and its association with Brugada syndrome (BrS). The proband experienced a life-threatening ventricular
Externí odkaz:
https://doaj.org/article/730a0eb7e9ed4593a39865012404112b
Autor:
Michelle M. Monasky, Emanuele Micaglio, Giuseppe Ciconte, Sara Benedetti, Chiara Di Resta, Gabriele Vicedomini, Valeria Borrelli, Andrea Ghiroldi, Marco Piccoli, Luigi Anastasia, Vincenzo Santinelli, Maurizio Ferrari, Carlo Pappone
Publikováno v:
Frontiers in Physiology, Vol 10 (2019)
Brugada syndrome (BrS) is a known cause of sudden cardiac death. The genetic basis of BrS is not well understood, and no one single gene is linked to even a majority of BrS cases. However, mutations in the gene SCN5A are the most common, although the
Externí odkaz:
https://doaj.org/article/369969c9aafc49dcaa36e59abf889efc
Autor:
Emanuele Micaglio, Michelle M. Monasky, Giuseppe Ciconte, Gabriele Vicedomini, Manuel Conti, Valerio Mecarocci, Luigi Giannelli, Federica Giordano, Alberto Pollina, Massimo Saviano, Simonetta Crisà, Valeria Borrelli, Andrea Ghiroldi, Sara D’Imperio, Chiara Di Resta, Sara Benedetti, Maurizio Ferrari, Vincenzo Santinelli, Luigi Anastasia, Carlo Pappone
Publikováno v:
Frontiers in Genetics, Vol 10 (2019)
In this case series, we report for the first time a family in which the inherited nonsense mutation [c. 3946C > T (p.Arg1316*)] in the SCN5A gene segregates in association with Brugada syndrome (BrS). Moreover, we also report, for the first time, the
Externí odkaz:
https://doaj.org/article/cc4522e886ff4e74a1f3698e9ba7eecd
Autor:
Carlo Pappone, MD, Gabriele Vicedomini, MD, Andrea Petretta, MD, Luigi Giannelli, MD, Amarild Cuko, MD, Vincenzo Santinelli, MD
Publikováno v:
HeartRhythm Case Reports, Vol 1, Iss 5, Pp 285-289 (2015)
Externí odkaz:
https://doaj.org/article/0f83939f26824a3ab8a2ab42060e6b50
Autor:
Giuseppe Ciconte, Antonio Boccellino, Gabriele Negro, Roberto Rondine, vincenzo maiolo, marco ballarotto, Antonio Napolano, valerio mecarocci, Luigi Giannelli, andrea cappabianca, Gabriele Vicedomini, Luigi Anastasia, Zarko Calovic, Vincenzo Santinelli, Carlo Pappone
Publikováno v:
Heart Rhythm. 20:S70-S71
Autor:
Carlo Pappone, Antonio Boccellino, Gabriele Negro, Roberto Rondine, Luigi Giannelli, valerio mecarocci, Zarko Calovic, Andrea Cappabianca, Vincenzo Maiolo, Antonio Napolano, Ludovico Sabatelli, marco ballarotto, Gabriele Vicedomini, Vincenzo Santinelli, Giuseppe Ciconte
Publikováno v:
Heart Rhythm. 20:S528
Autor:
Carlo Pappone, Giuseppe Ciconte, Vladimir Espinosa Angarica, Andrea Ghiroldi, Emanuele Micaglio, Pasquale Creo, Adriana Tarantino, Michelle Monasky, Marco Piccoli, Flavio Mastrocinque, Sara D'Imperio, Zarko Calovic, Antonio Boccellino, Federica Cirillo, Lorenzo Menicanti, Fiorenzo Gaita, Gabriele Vicedomini, Vincenzo Santinelli, Enrico Petretto, Luigi Anastasia
Publikováno v:
Heart Rhythm. 20:S264
Autor:
Carlo Pappone, Giuseppe Ciconte, Luigi Anastasia, Fiorenzo Gaita, Edward Grant, Emanuele Micaglio, Emanuela T Locati, Zarko Calovic, Gabriele Vicedomini, Vincenzo Santinelli
Publikováno v:
Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology.
Aims The long-QT syndrome (LQTS) represents a leading cause of sudden cardiac death (SCD). The aim of this study was to assess the presence of an underlying electroanatomical arrhythmogenic substrate in high-risk LQTS patients. Methods and results Th
Autor:
Enrico Petretto, Andrea Bernardini, Gabriele Vicedomini, Andrea Ghiroldi, Žarko Ćalović, Chiara Di Resta, Carlo de Innocentiis, Francesca Santini, Giuseppe Ciconte, Michelle M. Monasky, Valerio Mecarocci, Gabriele Negro, Giorgio Casari, Roberto Rondine, Luigi Giannelli, Beniamino C Mazza, Luigi Anastasia, Ilaria Rivolta, Sara Benedetti, Valeria Borrelli, Carlo Pappone, Vincenzo Santinelli, Emanuele Micaglio, Sara D'Imperio, Emanuela T Locati
Publikováno v:
European Heart Journal
Aims Brugada syndrome (BrS) is associated with an increased risk of sudden cardiac death due to ventricular tachycardia/fibrillation (VT/VF) in young, otherwise healthy individuals. Despite SCN5A being the most commonly known mutated gene to date, th